Microstructure of the silk spigots of the green crab spider Oxytate striatipes (Araneae: Thomisidae)

The genus Oxytate L. Koch, 1878 comprises a homogeneous group of nocturnal crab spiders that have silk apparatuses even though they do not spin webs to trap prey. We examined the microstructure of the silk spinning apparatus of the green crab spider Oxytate striatipes, using field emission scanning electron microscopy. The silk glands of the spider were classified into three types: ampullate, pyriform and aciniform. The spigots of these three types of silk gland occur in both sexes. Two pairs of major ampullate glands send secretory ductules to the anterior spinnerets, and another two pairs of minor ampullate glands supply the median spinnerets. In addition, the pyriform glands send ductules to the anterior spinnerets (45 pairs in females and 40 pairs in males), and the aciniform glands feed silk into the median (9–12 pairs in females and 7–10 pairs in males) and the posterior (30 pairs in both sexes) spinnerets. The spigot system of O. striatipes is simpler and more primitive than other wandering spiders: even the female spiders possess neither tubuliform glands for cocoon production nor triad spigots for web‐building.     

Microstructure of the silk apparatus in the coelotine spider Paracoelotes spinivulva (Araneae: Amaurobiidae)

The microstructural characteristics of the silk‐spinning apparatus and its ecological significance in the coelotine spider Paracoelotes spinivulva were examined by field emission scanning electron microscopy, with the goal of understanding the properties and the evolutionary origins of these silk constructs. The silk apparatuses of this spider were composed of four basic types of silk‐spinning spigot (ampullate, pyriform, aciniform and tubuliform), which connected with typical silk glands in the abdominal cavity. Of the three pairs of spinnerets, the posterior pairs were highly elongated along the body axis. Anterior spinnerets comprised two pairs of ampullate glands and approximately 70–80 pairs of pyriform glands in both sexes. Middle spinnerets had one to two pairs of ampullate spigots, three pairs of tubuliform spigots in females, and 50–60 (female) or 80–90 (male) pairs of aciniform spigots. An additional two pairs of tubuliform spigots in females and 70–80 (female) or 100–120 (male) pairs of aciniform spigots were counted on the spinning surfaces of the posterior spinnerets in both sexes. Although the coelotine spiders use their silk to catch prey, P. spinivulva characteristically do not have a typical “triad” spigot, including a flagelliform and two aggregate spigots, for capture thread production.     

The ontogeny of the spinning apparatus of Tengella perfuga (Araneae: Zoropsidae)

Silk is the most recognizable trait of spiders, and silk use has changed throughout spider evolutionary history. While morphology of the adult silk spigot has been a useful character for systematics, few studies have examined the ontogeny of the spinning apparatus, and none of these included cribellate spiders. Here, we report the first published full ontogeny of the spinning apparatus of a cribellate spider, Tengella perfuga. We found the presence of expected spigots: major ampullate gland and piriform gland spigots on the anterior lateral spinneret, minor ampullate gland and aciniform gland spigots on the posterior median spinneret, and aciniform gland spigots on the posterior lateral spinneret. Females, but not males, possessed cylindrical gland spigots on both the posterior median and lateral spinnerets. Spiderlings did not possess a functioning cribellum until the third instar. The cribellum grew with increasing numbers of spigots, but functionality was lost in adult males. Most intriguingly, second instars possessed a distinct triad of pre‐spigots on the posterior lateral spinneret. From the third instar onward, these structures formed the modified spigot along with two flanking spigots (in females) or formed nubbins (in males). We suggest that the modified spigot serves as the source of axial lines in the cribellate silk produced in T. perfuga. We also compare spigot ontogeny from previous studies of ecribellate spiders. These comparisons warrant further exploration using the recent spider tree of life in a phylogenetic comparative analysis of spigot ontogeny datasets, which could yield evidence for homologous spigots across the Araneomorphae, notably the Araneoidea and the Retrolateral Tibial Apophysis (RTA) clades.     

Microstructure of the silk apparatus of the comb-footed spider, Achaearanea tepidariorum (Araneae: Theridiidae)

The microstructural organization of the silk‐spinning apparatus of the comb‐footed spider, Achaearanea tepidariorum, was observed by using a field emission scanning electron microscope. The silk glands of the spider were classified into six groups: ampullate, tubuliform, flagelliform, aggregate, aciniform and pyriform glands. Among these, three types of silk glands, the ampullate, pyriform and aciniform glands, occur only in female spiders. One (adult) or two (subadult) pairs of major ampullate glands send secretory ductules to the anterior spinnerets, and another pair of minor ampullate glands supply the median spinnerets. Three pairs of tubuliform glands in female spiders send secretory ductules to the median (one pair) and posterior (two pairs) spinnerets. Furthermore, one pair of flagelliform glands and two pairs of aggregate glands together supply the posterior spinnerets, and form a characteristic spinning structure known as a “triad” spigot. In male spiders, this combined apparatus of the flagelliform and the aggregate spigots for capture thread production is not apparent, instead only a non‐functional remnant of this triad spigot is present. In addition, the aciniform glands send ductules to the median (two pairs) and the posterior spinnerets (12–16 pairs), and the pyriform glands feed silk into the anterior spinnerets (90–100 pairs in females and 45–50 pairs in males).     

Spinneret Microstructure of the Silk Spinning Apparatus in the Crab Spider, Misumenops tricuspidatus (Araneae: Thomisidae)

The silk spinning apparatus in the crab spider, Misumenops tricuspidatus was studied with the field emission scanning electron microscope (FESEM) and the main microstructural characteristics of the silk glands are presented. In spite of the fact that the crab spiders do not spin webs to trap a prey, they also have silk apparatus even though the functions are not fully defined. The crab spider, Misumenops tricuspidatus possesses only three types of silk glands which connected through the typical spinning tubes on the spinnerets. The spinning apparatus of Misumenops closely corresponds to that of wandering spiders such as jumping spiders or wolf spiders except some local variations. Anterior spinnerets comprise 2 pairs of the ampullates and 48 (±5) pairs of pyriform glands. Another 2 pairs of ampullate glands and nearly 20 (±3) pairs of aciniform glands were connected on the middle spinnerets. Additional 50 (±5) pairs of the aciniform glands were connected on the posterior spinnerets. The aggregate glands and the flagelliform glands which have the function of sticky capture thread production in orb‐web spiders as well as the tubuliform glands for cocoon production in females were not developed at both sexes of this spider, characteristically.     

Fine Structural Analysis of the Silk Apparatus in the Funnel-web Spider, Agelena limbata (Araneae: Agelenidae)

ABSTRACT Silk apparatus of the funnel-web spider, Agelena limbata was located at the ventral end of the abdominal part, and was composed of internal silk glands and external spinnerets. Among the three pairs of spinnerets, the posterior pairs were highly elongated along the body axis. By the light and electron microscopic inspections, it was found that four types of silk glands were connected through the typical spinning tubes of each spinneret. Anterior spinnerets comprise 2 pairs of the ampullate and 125 to 150 pairs (female) or 110 to 114 (male) of pyriform glands. Another 2 pairs of ampullate glands in both sexes, 5 to 8 pairs of tubuliform glands in females, and 20 to 26 pairs (female) or 15 to 17 pairs (male) of aciniform glands were connected on the median spinnerets. Additional 8 to 10 pairs of tubuliforms in female and 41 to 53 pairs (female) or 27 to 32 pairs (male) of aciniform glands were on the posterior spinnerets, respectively. While the ampullate and tubuliform glands were connected with the spigot-type spinning tubes, the pyriform and aciniform glands with that of spool-type tubes. It has been also revealed that the tubuliform glands were only observed in female spiders, however the flagelliform and aggregate glands which had the function of adhesive thread production in orb-web spiders were not observed at both sexes of this spiders.     

The spinning apparatus of Polenecia producta (Araneae,Uloboridae): Structure and histochemistry

Summary The spinning apparatus of the uloborid spider Polenecia producta was studied to complete previous studies on the same family of spiders. The structure of spinnerets and spigots, under scanning electron microscopy, and the main anatomical and histochemical characteristics of the spinning glands of adult females and males are described. In addition some observations on the spinning apparatus at three successive stages of development are made. There are nine kinds of silk glands in Polenecia, i.e. one more (aciniform — B glands) than found in other uloborids. The spinning apparatus of Polenecia is, therefore, the most complex so far known. It is also more complex than that presently known of Araneoidea. The characteristics of the spinning glands of Polenecia are compared with those of other uloborids. Present knowledge of the spinning apparatus of uloborids leads to a renewed discussion of the origin of the orb web in this family and in araneids. It is concluded that these two types of orb webs emerged from independent evolutionary processes.     

Functional organization of the spinning apparatus of Cyrtophora citricola with regard to the evolution of the web (Araneae,Araneidae)

Summary The spinning apparatus of Cyrtophora citricola closely corresponds to that of orb-weaving Araneidae, two peculiarities excepted. Firstly the spigots of the piriform glands differ extremely in size, the smallest of them being numerous and having a unique location on the anterior spinnerets. Secondly, the triad complex (on the posterior spinnerets) used by other Araneidae for producing gluey capture threads is lacking. Both these characteristics are correlated with the construction of a fine meshed sheet of dry silk by Cyrtophora instead of orbwebs with capture spirals. The sheet can be understood as being a very much enlarged central area of orb-webs. Since vestiges of triads could be found in early developmental stages of C. citricola, the origin of the meshed sheet from orb-webs with gluey capture threads is clearly demonstrated. The paper includes a study on how the spider produces thread attachments by means of the secretions of the piriform glands.     

A new mechanosensory organ on the anterior spinnerets of the spiderCupiennius salei (Araneae,Ctenidae)

We describe hitherto unknown mechanoreceptors on the anterior spinnerets of the spiderCupiennius salei. These receptors are found at the base of the spigots of the major ampullate glands which produce the dragline used by the spider as a safety thread in various behavioral situations. There are 40–60 mechanoreceptors associated with two spigots of each anterior spinneret. They are likely to provide information on the forces pulling on the dragline and also on its orientation in space. A single sensillum consists of a hole in the cuticle covered by a thin cuticular membrane. It much resembles spider slit sensilla, which are known to detect strains in the exoskeleton. Each sensillum is supplied by two dendrites most likely belonging to two bipolar sensory cells. One of the dendrites ends at the covering membrane and the other more proximally. The sensilla are arranged with their long axes roughly parallel to the circumference of the spigots. External forces, transmitted by the dragline, result in deformation of the central part of the cuticular plate at the base of the spigots and thus in stimulation of the sensilla. This is shown electrophysiologicallly. Considering their morphology, topography, and electrophysiology, these mechanoreceptors are suggested to be important in the sensory control of dragline release by the spider.     

Lyriform slit sense organs on the pedipalps and spinnerets of spiders

Lyriform slits sense organs (LSSO) are a precise assembly of stress detecting cuticular slit sensilla found on the appendages of arachnids. While these structures on the legs of the wandering spiderCupennius salei are well studied in terms of morphology, function and contribution to behaviour, their distribution on pedipalps and spinnerets of spiders is not well explored. A study was therefore carried out to observe the distribution of LSSO on pedipalps and spinnerets of some spider species. Haplogyne spiders belonging to familyPholcidae have a simple complement of LSSOs represented by one or two LSSOs on their femur. The entelegyne spiders possess a complex assembly of LSSOs on the distal segments of their pedipalps. Various types of LSSOs are found on the pedipalps indicating a capacity for analysis of complex cuticular stress. It is suggested that the complexity of LSSOs on pedipalps of entelegyne spiders relates to courtship and spermatophore transfer and may help in reproductive isolation. Lack of LSSOs on the distal segments of pedipalps leads us to infer that unlike legs, pedipalps are less likely to receive vibratory input through their distal segments. Spinnerets have a relatively simple complement of LSSOs. One LSSO is found only on anterior spinnerets and it is a common feature observed among spiders, irrespective of the variations in web building behaviour. The orb-weaving araneidArgiope pulchella, however, has two LSSOs on the anterior spinneret. As non-web builders and orb weavers do not differ markedly in terms of LSSOs on the spinnerets and LSSOs are simple in nature (type A), it is likely that spinning and weaving are not largely regulated by sensory input from LSSOs on the spinnerets.     

Alleged silk spigots on tarantula feet: Electron microscopy reveals sensory innervation,no silk

Several studies on tarantulas have claimed that their tarsi could secrete fine silk threads which would provide additional safety lines for maintaining a secure foot-hold on smooth vertical surfaces. This interpretation was seriously questioned by behavioral experiments, and more recently morphological evidence indicated that the alleged spigots (“ribbed hairs”) were not secretory but most likely sensory hairs (chemoreceptors). However, since fine structural studies were lacking, the sensory nature was not proven convincingly. By using transmission electron microscopy we here present clear evidence that these “ribbed hairs” contain many dendrites inside the hair lumen – as is the case in the well-known contact chemoreceptors of spiders and insects. For comparison, we also studied the fine structure of regular silk spigots on the spinnerets and found them distinctly different from sensory hairs. Finally, histological studies of a tarantula tarsus did not reveal any silk glands, which, by contrast, are easily found within the spinnerets. In conclusion, the alleged presence of silk spigots on tarantula feet is refuted.     

The morphology and relationships of the walking mud spiders of the genus Cryptothele (Araneae: Zodariidae)

We revise the relationships of the spider genus Cryptothele after reexamination of the morphology of the spinnerets, leg tarsal claws and maxillae with scanning electron microscopy. Cryptothele species have a particular conformation of the spinning field of the anterior lateral spigots that is typical of zodariids and close relatives: the field of major ampullate gland spigots, together with their strain sensilla, are invaginated within the field of piriform gland spigots. The implantation of the teeth on the inner side of the leg tarsal claws is also consistent with its placement among zodariids. We added Cryptothele to a morphological dataset of zodariid genera, together with the outgroups Homalonychus (Homalonychidae) and Penestomus (Penestomidae). The phylogenetic analysis concludes that the genus Cryptothele is a member of the subfamily Cydrelinae, which by priority is here considered a junior synonym of Cryptothelinae. Cryptothele specimens cover most of their body with soil particles which become consolidated as mud, and the debris is probably held in place by curved setae covered by long barbs. The spinnerets, which can be retracted and hidden, as well as the booklungs, are surrounded by a crown of thick setae that are densely covered by short barbs, protecting those areas against soil particles. Cryptothele are probably specialized to prey on termites, and their phylogenetic placement indicates that this diet specificity evolved two times independently in zodariids.     

The spinnerets and epiandrous glands of spiders

The spinnerets of spiders are carried on the fourth and fifth segments of the abdomen (opisthosoma). Primitively there are two pairs, anterior lateral ( al ) and anterior median ( am ) on the fourth segment, and two pairs, posterior lateral ( pl ) and posterior median ( pm ) on the fifth, am are present in Liphistius but are never functional. In mygalomorphs am are invariably absent, and usually al also. In araneomorphs am are either reduced to a function-less colulus, perhaps absent altogether, or represented by the cribellum, which is a specialized spinning organ.
It seems unlikely that the lateral and median spinnerets correspond to the exopodites and endopodites of a biramous limb, which limbs are characteristic of the Crustacea, a group having no close relationship to the Arachnida. From embryology it seems clear that the lateral spinnerets are the segmental appendages. Glands, here described as the epiandrous glands, very similar to spinning glands, occur on the second abdominal segment of most male spiders. It is suggested that these may be serially homologous with the median spinnerets, which would then not be appendicular in origin but would be modifications of ventral glandular structures.     

On the spinning apparatus and the structure of the capture threads ofDeinopis subrufus (Araneae,Deinopidae)

Summary The spinnerets and spigots of two adult femaleDeinopis subrufus and one adult male were studied with the scanning electron microscope. The organization of the spinning apparatus corresponds very closely to that of Uloboridae. The capture threads produced by the male while subadult were studied with the light microscope and with the SEM. This study includes the questions of the glandular origin and the functions of the components of these threads. A hypothesis for howD. subrufus constructs capture threads is proposed.     

Spiders spinning electrically charged nano-fibres

Most spider threads are on the micrometre and sub-micrometre scale. Yet, there are some spiders that spin true nano-scale fibres such as the cribellate orb spider, Uloborus plumipes. Here, we analyse the highly specialized capture silk-spinning system of this spider and compare it with the silk extrusion systems of the more standard spider dragline threads. The cribellar silk extrusion system consists of tiny, morphologically basic glands each terminating through exceptionally long and narrow ducts in uniquely shaped silk outlets. Depending on spider size, hundreds to thousands of these outlet spigots cover the cribellum, a phylogenetically ancient spinning plate. We present details on the unique functional design of the cribellate gland–duct–spigot system and discuss design requirements for its specialist fibrils. The spinning of fibres on the nano-scale seems to have been facilitated by the evolution of a highly specialist way of direct spinning, which differs from the aqua-melt silk extrusion set-up more typical for other spiders.     

Developmental changes in the spinning apparatus over the life cycle of wolf spiders (Araneae: Lycosidae)

Spiders are characterized by their spinning activity. Much of the current knowledge of the spinning apparatus comes from studies on orb web spiders and their relatives, whereas wolf spiders have been more or less neglected in this respect. Therefore, we studied developmental changes in the spinning apparatus of four wolf spiders (Tricca lutetiana, Arctosa alpigena lamperti, Pardosa amentata, and Xerolycosa nemoralis) throughout their life cycles. Each of these lycosids has a stenochronous life cycle, but of varied length (from 1 to 3 years) and number of instars (from seven to ten). Use of the spinning apparatus begins in the first instar, after leaving the egg sac. Secondary ampullate, all piriform, and all but four aciniform glands are tartipore‐accommodated. The tartipores, collared openings through which silk gland ducts pass during proecdysis, appear on the spinning field starting with the second instar. Tartipore‐accommodated glands can function during proecdysis and their evolution corresponds with the way spiders secure themselves when molting. We suggest that the function of aciniform silk in juvenile wolf spiders is to serve as an ancillary “scaffold” supporting the spider's body during ecdysis.     

Structure and cytochemistry of the silk glands of the mygalomorph spider Antrodiaetus unicolor (araneae,antrodiaetidae)

Dissection and a variety of absorption and fluorescent cytochemical methods have demonstrated that Antrodiaetus unicolor females have only one type of silk gland and spigot and, consequently, the simplest silk production system of any spider yet investigated histochemically. The small spherical to pear-shaped glands are grouped into four clusters, each cluster serving one of the four spinnerets. The spigots are long, slender, and slightly bent distally. Although all gland cells are structurally similar, each gland simultaneously produces two different secretory products, the secretion of the distal hemisphere being rich in basic protein and sulfhydryl groups, and the proximal hemisphere secretion being an acidic protein containing a high concentration of histochemically demonstrable C-terminal carboxyl groups. The two products remain segregated as they pass through the duct, where the acidic protein forms a thin outer layer around a core of basic protein. It is suggested that this segregation may persist in the silk strand after it exits from the spigot and that the outer acidic protein may be an adhesive agent.     

Almost a spider: a 305-million-year-old fossil arachnid and spider origins

Spiders are an important animal group, with a long history. Details of their origins remain limited, with little knowledge of their stem group, and no insights into the sequence of character acquisition during spider evolution. We describe a new fossil arachnid, Idmonarachne brasieri gen. et sp. nov. from the Late Carboniferous (Stephanian, ca 305–299 Ma) of Montceau-les-Mines, France. It is three-dimensionally preserved within a siderite concretion, allowing both laboratory- and synchrotron-based phase-contrast computed tomography reconstruction. The latter is a first for siderite-hosted fossils and has allowed us to investigate fine anatomical details. Although distinctly spider-like in habitus, this remarkable fossil lacks a key diagnostic character of Araneae: spinnerets on the underside of the opisthosoma. It also lacks a flagelliform telson found in the recently recognized, spider-related, Devonian–Permian Uraraneida. Cladistic analysis resolves our new fossil as sister group to the spiders: the spider stem-group comprises the uraraneids and I. brasieri. While we are unable to demonstrate the presence of spigots in this fossil, the recovered phylogeny suggests the earliest character to evolve on the spider stem-group is the secretion of silk. This would have been followed by the loss of a flagelliform telson, and then the ability to spin silk using spinnerets. This last innovation defines the true spiders, significantly post-dates the origins of silk, and may be a key to the group''s success. The Montceau-les-Mines locality has previously yielded a mesothele spider (with spinnerets). Evidently, Late Palaeozoic spiders lived alongside Palaeozoic arachnid grades which approached the spider condition, but did not express the full suite of crown-group autapomorphies.